Combining Desferriferrioxamine B and 1-Hydroxy-2-Piperidone ((PIPO)H) to Chelate Zirconium. Solution Structure of a Model Complex of the [Zr]Zr-DFOcyclo*-mAb Radioimmunoconjugate.

Fiche publication

Date publication

juillet 2024

Journal

ChemPlusChem

Auteurs

Membres identifiés du Cancéropôle Est :
Dr CHAMBRON Jean-Claude

Tous les auteurs :
Mangin F, Fonquernie O, Jewula P, Brandès S, Penouilh MJ, Bonnin Q, Vincent B, Espinosa E, Aubert E, Meyer M, Chambron JC

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/38613508

Résumé

Zr-immunoPET is a hot topic as Zr cumulates the advantages of Cu and I without their drawbacks. We report the synthesis of a model ligand of a chiral bioconjugable tetrahydroxamic chelator combining the desferriferrioxamine B siderophore and 1-hydroxy-2-piperidone ((PIPO)H), a chiral cyclic hydroxamic acid derivative, and the study by NMR spectroscopy of its zirconium complex. Nuclear Overhauser effect measurements (ROESY) indicated that the complex exists in the form of two diastereomers, in 77 : 23 ratio, resulting from the combination of the central chiralities at the 3-C of the (PIPO)H component and at the Zr cation. The 44 lowest energy structures out of more than 1000 configurations/conformations returned by calculations based on density functional theory were examined. Comparison of the ROESY data and the calculated interatomic H⋅⋅⋅H distances allowed us to select the most probable configuration and conformations of the major complex.